Canonical Allele Identifier: PA2827680055
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 2942872
ClinVar RCV Id: RCV003808038

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339705.1:p.Met89Lys
CA399505773
NM_001352776.2:c.266T>A